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Öğe A child with glomangioma and osteochondroma on the same leg: A case report(2008) Köksal Y.; Çalişkan U.; Reisli I.; Uçar C.; Avunduk M.C.Glomangioma is a rare neoplasm that typically occurs in soft tissue of the extremities, particularly the subungual region of the fingertip. Osteochondromas are benign proliferations composed of mature bone and a cartilaginous cap. A case involving a 9-year-old boy with two benign masses (glomangioma and osteochondroma) on his right leg is presented. To our knowledge, this is the first case of glomangioma associated with osteochondroma in a child that has been reported.Öğe Clinical and laboratory features in pediatric patients with common variable immunodeficiency [De?işken immün yetersizlikli çocuk hastalarda klinik ve laboratuvar özellikler](Kare Publishing, 2007) Artaç H.; Keleş S.; Kara R.; Reisli I.Aim: Common variable immunodeficiency (CVID) is a primary immunodeficiency disease characterized by defective antibody production and heterogeneous clinical features. We aimed to describe clinical and laboratory features of our patients with CVID. Materail and Method: We restrospectively evaluated the records of children diagnosed with CVID from February 2002 to June 2006 and followed-up for a mean of 29.7±17.4 (2-51) months. Results: A total of 10 patients, 7 females and 3 males (mean age: 9.4±5.1, ranging from 3 to 18) were included in this study. All of them were admitted to our clinic due to recurrent bronchopneumonia. Nine patients had chronic pulmonary disease at the time of CVID diagnosis and lobectomy had been performed in three patients. Serum IgG concentrations were less than 200 mg/dl in four patients. There was a reduction of at least two serum immunoglobulin levels in six patients. Four patients had normal IgG levels, but two of them had decreased IgM levels and the other two had decreased IgA levels. The percentages of B cells was found to be low (%1.6-8.9; 5.3±2.8) in all of the patients. The inversion in the CD4/CD8 ratio was observed in the peripheral blood lymphocytes of eight patients. Conclusions: We suggested that CVID should be especially investigated in patients with chronic pulmonary disease.Öğe The clues of the primary immunodeficiency in newborn [Yenido?an bebekte immün yetersizli?in ipuçlari](2007) Reisli I.The specific antibodies were low in sera of the neonates with no immunological memory and low ability to develop specifik antibody. Defense against infection in neonate is predominantly dependent on innate immunity. Because the functional capacity of the other compartments of the immune system is insufficient, the newborns have a higher frequency of infections than older children and adults. It is an important issue to know the some clues such as a family history of immunodeficiency, late separation of umblical cord, lymphopenia, moniliasis, absence of peripheral lymphoid tissue, organ abscesses and hypocalsemic tetani that indicate immunodeficiency in a newborn with insufficient immune system. It is possible to determine this clues with an adequate history, well-done physical examination and a careful clinical follow up.Öğe A multiple myeloma case presenting with bilateral pleural involvement [Bilateral plevral tutulum ile başvuran multipl miyelom olgusu](2007) Yosunkaya Ş.; Maden E.; Toy H.; Yazici R.; Özer F.; Reisli I.Pleural effusion is a relatively infrequent finding in multiple myeloma (MM) and malign effusions due to myelomatous effusion is seen very rarely. In this article we reported a case with bilateral myelomatous effusion. Myelomatous etiology was detected by demonstrating gammopaty in pleural fluid protein electrophoresis and demonstrating abundant number of atypical plasma cells in pleural fluid cytology. Pleural fluids due to MM are usually seen in IgA type of MM's, IgG on the surface of CD-138 positive cell was demonstrated in flow cytometric study of the pleural fluid of the reported case. In conclusion we mentioned that a patient who does not have diagnosis of MM before may present with pleural involvement, the involvement may be bilateral and flow cytometry can be used in diagnosis.Öğe Pulmonary vascular sling with aberrant right upper lobe pulmonary artery in a child(2003) Başpinar O.; Karaaslan S.; Oran B.; Reisli I.; Keleş S.; Baysal T.[Abstract not Available]Öğe Three Cases with Langerhans Cell Histiocytosis with Sistemic Involvement [Sistemik Tutulum ile Giden Langerhans Hücreli Histiositozis'li Üç Vaka Sunumu](2004) Köksal Y.; Gülyüz A.; Çalişkan Ü.; Reisli I.; Uçar C.Histiocytosis which is a proliferative process characterized by an accumulation of dentritic cells in various tissues and organs is a rare disease. It can occur as an isolated lesion or as widespread systemic disease involving virtually any body site. Langerhans cell histiocytosis was diagnosed by light microscopy in a 27-month-old boy and 16-month-old girl with anemia hepatosplenomegaly, exanthema and lesions on the skull and a 9-month-old girl with thymic and cutaneous involvement. Clinical and laboratory findings of the cases are discussed in the light of literature.
